Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
NA
30 participants
INTERVENTIONAL
2022-09-01
2024-12-31
Brief Summary
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The anomaly of teething, first of all, affects the anatomical, functional and aesthetic characteristics, there is an influence on the psycho-emotional state of the patient. Despite a significant number of scientific studies by domestic and foreign authors, some features of the treatment of patients with dental retention are insufficiently covered and systematized. At the moment, there is no optimal approach to the diagnosis and treatment of dental retention, as a result of which there is a question of improving the effectiveness and quality of orthodontic treatment of patients with a diagnosis of "tooth retention".
Detailed Description
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1. To determine the frequency of occurrence of dental retention according to the patients' requests for orthodontic care;
2. Based on the cephalometric study to identify the features of the structure of the face and bone structures in patients with dental retention;
3. Develop and implement an orthodontic device to obtain additional space in the dentition in patients with retention;
4. To develop and introduce into clinical practice a method for creating surgical access to retentive teeth using digital technologies.
5. To conduct a comparative analysis of the effectiveness of our proposed improved stages of treatment of patients with dental retention with well-known methods based on gnatic and profilometric indicators.
Materials and methods of research At the first stage of our study, it is planned to examine patients aged 15-35 years who have applied for specialized
Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
At the second stage of our study, it is planned to sample the results with the division of patients into the main and control groups. The main group will include patients who will receive orthodontic treatment according to the method we have proposed. The control group will include patients whose treatment will be carried out according to the standard method
TREATMENT
NONE
Study Groups
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main group
This group consists of patients with dental retention who will be treated using digital technologies and devices to create a place in the dentition
exposure of the tooth crown
surgical exposure of the crown of a retentive tooth
Interventions
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exposure of the tooth crown
surgical exposure of the crown of a retentive tooth
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
15 Years
25 Years
ALL
No
Sponsors
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Samara State Medical University
OTHER
Responsible Party
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Locations
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Irina
Samara, Samara Oblast, Russia
Countries
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Other Identifiers
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8
Identifier Type: -
Identifier Source: org_study_id